25 results · 21ms · Sources: EU EUDAMED, US FDA

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SENSITITRE 18-24 HR SUSCEPTIBILITY PLATES

FDA 510(k)
FDA Class 2 ·Microbiology

SOL-M™ Hypodermic Needle

FDA UDI
Sol-Millennium Medical, Inc.·00818392016116·SOL-M Hypodermic Needle 16G*1 1/2

DD tempMED

FDA UDI
Dental Direkt GmbH·EDDIK111151·DD tempMED are pre-colored dental milling blank...

DD tempMED

FDA UDI
Dental Direkt GmbH·EDDIK116151·DD tempMED are pre-colored dental milling blank...

Meridian

FDA UDI
Seaspine Orthopedics Corporation·10889981214906·Interbody, 35mm x 27mm x 16mm, 15 Deg

3D Printed Interbody System

FDA UDI
Seaspine Orthopedics Corporation·10889981303556·Interbody, 35mm x 27mm x 16mm, 15 Deg, 3D

MicroSelectron Digital

FDA UDI
Nucletron B.V.·08717213026209·microSelectron Transfer Tube for 5F Flexibles (19)

Sklar®

FDA UDI
SKLAR CORPORATION·10649111167980·STILLE PLASTER SHEARS 2 HND 15

Meridian

FDA UDI
Seaspine Orthopedics Corporation·10889981216801·Trial, 35mm x 27mm x 16mm, 15 Deg

Biopsy Forceps

FDA UDI
ENDO-THERAPEUTICS, INC.·00816207020730·Endoscopic Biopsy Forceps

Biopsy Forceps

FDA UDI
ENDO-THERAPEUTICS, INC.·00816207020778·Endoscopic Biopsy Forceps

WATER FILLED TEETHER, WATER FILLED TEETHER WITH HANDLE

FDA 510(k)
FDA Class 2 ·Dental

POWERWIRE RADIOFREQUENCY GUIDEWIRE

FDA 510(k)
FDA Class 2 ·Cardiovascular

¿ZENAPRO HYBRID HERNIA REPAIR GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code FTL·September 23, 2015

VASO VIEW HEMOPRO

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·May 6, 2013

UNKNOWN DEPUY PINNACLE 52MM CUP

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·May 13, 2011

MTS A/B/D MONOCLONAL AND REVERSE GROUPING CARD

FDA Adverse Event
Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·August 13, 2008

ACTIVA

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·June 24, 2020

ULTRASAFE X100L PNG TEAL NVS STEIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·October 7, 2020

ZENAPRO HYBRID HERNIA REPAIR GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH, INC.·Product code FTL·August 8, 2014